Clinical and Paraclinical Characteristics of Severe Bronchiolitis in Children From 2 Months to 12 Months at the Children's Hospital 1 in Ho Chi Minh City - Vietnam
- Conditions
- Epidemiological, Clinical, Paraclinical Characterictics of Severe Bronchiolitis
- Interventions
- Biological: severe bronchiolitis
- Registration Number
- NCT04174430
- Lead Sponsor
- University of Medicine and Pharmacy at Ho Chi Minh City
- Brief Summary
Goal: The aim of this study is to determine the epidemiological, clinical, paraclinical characteristics and treatment of severe bronchiolitis at the Children Hospital N01 in 2001-2002.
Materials and method: in this cross-sectional study, specimens of 51 patients with severe bronchiolitis at the Children Hospital N01 from March, 1 st 2001 to February, 28th 2002 are described and analyzed.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- UNKNOWN
- Sex
- All
- Target Recruitment
- 51
- children younger from 2-12 months present fever (usually ≤38.3ºC [101ºF]) ,cough, and respiratory distress (eg, increased respiratory rate, retractions, wheezing, crackles)
- preceded by a one- to three-day history of upper respiratory tract symptoms (eg, nasal congestion and/or discharge) ]
- Respiratory distress.
- refusal to give informed consent
- mucus sample Barlett <=0
Study & Design
- Study Type
- OBSERVATIONAL
- Study Design
- Not specified
- Arm && Interventions
Group Intervention Description mild to moderate bronchiolitis severe bronchiolitis Bronchiolistis patients without Prematurity (gestational age ≤36 weeks), Low birth weight, Age less than 12 weeks, Chronic pulmonary disease, particularly bronchopulmonary dysplasia (also known as chronic lung disease), Anatomic defects of the airways, Hemodynamically significant congenital heart disease, Immunodeficiency and Neurologic disease
- Primary Outcome Measures
Name Time Method Number of participants with Severe bronchiolitis at the Children Hospital N01 2 years Bronchiolitis in infants with:
* Preterm birth : gestational age \< 37 weeks
* Respiratory failure:
* Irritable condition
* Breath rate \> 50 per minute
* Hypoxiemia: SpO2 \< 94%
* Poor feeding
* Hemodynamically significant congenital heart disease (congennital heart failure, moderate to severe pulmonary hypertension or cyanotic heart disease)
- Secondary Outcome Measures
Name Time Method
Trial Locations
- Locations (1)
Respiratory
🇻🇳Ho Chi Minh City, District 10, Vietnam